List of variants reported as likely pathogenic for Fanconi anemia complementation group C by Myriad Genetics, Inc.

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.1642C>T (p.Arg548Ter)	rs104886457	0.00007
NM_000136.3(FANCC):c.996+1G>T	rs370510954	0.00001
NM_000136.3(FANCC):c.1029C>A (p.Tyr343Ter)	rs2072504418
NM_000136.3(FANCC):c.1029C>G (p.Tyr343Ter)
NM_000136.3(FANCC):c.1084G>T (p.Gly362Ter)	rs2072245226
NM_000136.3(FANCC):c.225T>A (p.Cys75Ter)
NM_000136.3(FANCC):c.249T>A (p.Tyr83Ter)
NM_000136.3(FANCC):c.275G>A (p.Trp92Ter)	rs1830584796
NM_000136.3(FANCC):c.282_283del (p.Cys95fs)
NM_000136.3(FANCC):c.315_316insCCCG (p.Gly106fs)
NM_000136.3(FANCC):c.323C>A (p.Ser108Ter)	rs1830581816
NM_000136.3(FANCC):c.353T>A (p.Leu118Ter)	rs1825725461
NM_000136.3(FANCC):c.464T>A (p.Leu155Ter)	rs1825652774
NM_000136.3(FANCC):c.560del (p.Cys187fs)
NM_000136.3(FANCC):c.661G>T (p.Glu221Ter)	rs1830059125
NM_000136.3(FANCC):c.683dup (p.Leu228fs)
NM_000136.3(FANCC):c.793G>T (p.Glu265Ter)	rs1827526425
NM_000136.3(FANCC):c.822C>A (p.Cys274Ter)

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